Benzoic acid (S)-3-((S)-2-tert-butoxycarbonylamino-propionylamino)-1-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethyl)-2,5-dioxo-pyrrolidin-3-ylmethyl ester

Base Information

Chemical Name:Benzoic acid (S)-3-((S)-2-tert-butoxycarbonylamino-propionylamino)-1-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethyl)-2,5-dioxo-pyrrolidin-3-ylmethyl ester
CAS No.:182176-34-7
Molecular Formula:C₃₅H₄₄N₄O₈
Molecular Weight:648.756
Hs Code.:

Benzoic acid (S)-3-((S)-2-tert-butoxycarbonylamino-propionylamino)-1-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethyl)-2,5-dioxo-pyrrolidin-3-ylmethyl ester

Synonyms:Benzoic acid (S)-3-((S)-2-tert-butoxycarbonylamino-propionylamino)-1-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethyl)-2,5-dioxo-pyrrolidin-3-ylmethyl ester

Suppliers and Price of Benzoic acid (S)-3-((S)-2-tert-butoxycarbonylamino-propionylamino)-1-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethyl)-2,5-dioxo-pyrrolidin-3-ylmethyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of Benzoic acid (S)-3-((S)-2-tert-butoxycarbonylamino-propionylamino)-1-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethyl)-2,5-dioxo-pyrrolidin-3-ylmethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Benzoic acid (S)-3-((S)-2-tert-butoxycarbonylamino-propionylamino)-1-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethyl)-2,5-dioxo-pyrrolidin-3-ylmethyl ester

There total 5 articles about Benzoic acid (S)-3-((S)-2-tert-butoxycarbonylamino-propionylamino)-1-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethyl)-2,5-dioxo-pyrrolidin-3-ylmethyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 86.0%

: 15761-38-3
L-N-Boc-Ala

: 182176-32-5
Benzoic acid (S)-3-amino-1-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethyl)-2,5-dioxo-pyrrolidin-3-ylmethyl ester

: 182176-34-7
Benzoic acid (S)-3-((S)-2-tert-butoxycarbonylamino-propionylamino)-1-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethyl)-2,5-dioxo-pyrrolidin-3-ylmethyl ester

Guidance literature:: With 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; for 2h; Ambient temperature;
DOI:10.1002/hlca.19960790508

Reference yield:

: 17186-53-7,92698-80-1
L-phenylalanine cyclohexylamide

: 182176-34-7
Benzoic acid (S)-3-((S)-2-tert-butoxycarbonylamino-propionylamino)-1-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethyl)-2,5-dioxo-pyrrolidin-3-ylmethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 43 percent / Et(i-Pr)2N / various solvent(s) / 32 h / 80 °C / in NMP

2: 1.) CF₃COOH 2.) SOCl₂ / 1.) CH₂Cl₂, r.t., 5 h 2.) CH₂Cl₂, r.t., 15 h

3: 87 percent / 2 N HCl / dioxane / 3 h / Ambient temperature

4: 86 percent / HATU, HOAT, Et(i-Pr)2N / dimethylformamide / 2 h / Ambient temperature

With hydrogenchloride; thionyl chloride; 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1002/hlca.19960790508

Reference yield:

: (4-Iodomethyl-5-oxo-2-phenyl-4,5-dihydro-oxazol-4-yl)-acetic acid tert-butyl ester

: 182176-34-7
Benzoic acid (S)-3-((S)-2-tert-butoxycarbonylamino-propionylamino)-1-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethyl)-2,5-dioxo-pyrrolidin-3-ylmethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 43 percent / Et(i-Pr)2N / various solvent(s) / 32 h / 80 °C / in NMP

2: 1.) CF₃COOH 2.) SOCl₂ / 1.) CH₂Cl₂, r.t., 5 h 2.) CH₂Cl₂, r.t., 15 h

3: 87 percent / 2 N HCl / dioxane / 3 h / Ambient temperature

4: 86 percent / HATU, HOAT, Et(i-Pr)2N / dimethylformamide / 2 h / Ambient temperature

With hydrogenchloride; thionyl chloride; 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1002/hlca.19960790508